ClinVar Miner

Submissions for variant NM_004992.3(MECP2):c.1162_1179del (p.Pro388_Pro393del) (rs267608406)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000488269 SCV000575668 uncertain significance not provided 2018-09-30 criteria provided, single submitter clinical testing
GeneDx RCV000132922 SCV000565121 benign not specified 2015-08-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000645134 SCV000766876 likely benign Severe neonatal-onset encephalopathy with microcephaly 2017-11-17 criteria provided, single submitter clinical testing
RettBASE RCV000132922 SCV000187903 benign not specified 2011-11-01 no assertion criteria provided curation

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.